How many moles of sulfur will be needed to oxidize 3 moles of zinc to zinc sulfide
1 answer:
Answer : The number of moles of sulfur needed to oxidize will be, 3 moles
Solution : Given,
Moles of zinc = 3 moles
The balanced reaction will be,
By the stoichiometry, 1 mole of ion react with the 1 mole of
to give 1 mole of zinc sulfide.
From the balanced reaction, we conclude that
As, 1 mole of zinc react with 1 mole of sulfur
So, 3 moles if zinc react with 3 moles of sulfur
Hence, the number of moles of sulfur needed to oxidize will be, 3 moles
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Answer: Option (4) is the correct answer.
Explanation:
When sulfuric acid reacts with calcium hydroxide then it results in the formation of calcium sulfate and water.
The chemical reaction for the same will be as follows.
Thus, we can conclude that salt is produced when sulfuric acid and calcium hydroxide react completely.
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.